Hematologic Diseases Clinical Trial
Official title:
The Use of Residual De-identified Specimens and/or Samples From Patients for Clinical Research
Acquire residual human specimens and/or samples from patient samples which were sent for testing at LabPMM, LLC for Clinical Research
| Status | Not yet recruiting |
| Enrollment | 2000 |
| Est. completion date | June 30, 2027 |
| Est. primary completion date | March 30, 2027 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: 1. Specimen/sample, peripheral blood (PB), bone marrow (BM), genomic DNA (gDNA) and/or formalin-fixed paraffin-embedded tissue (FFPE) from patients whose specimens/samples have been sent to LabPMM for clinical testing 2. Donor Age = 18 years Exclusion Criteria: 1. Sample/specimen has been obtained from a third-party vendor with a Materials Transfer Agreement (MTA) on file with LabPMM 2. The specimens/samples have previously been enrolled in a clinical study |
| Country | Name | City | State |
|---|---|---|---|
| United States | LabPMM | San Diego | California |
| Lead Sponsor | Collaborator |
|---|---|
| Invivoscribe, Inc. |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Enrollment | N=2000 | 3 years |
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